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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459715Generated: October 26, 2026

Triethylamine → 4-(5-Oxazolyl)-benzamide

https://huagongshe.com/reaction/459715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium HydroxideHCID 14923—
ReactantIsobutyl chloroformateHCID 62365—
Reactant4-(1,3-Oxazol-5-yl)benzoic AcidHCID 2776414—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Oxazolyl)-benzamideHCID 2193099948.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-(5-oxazolyl)benzoic acid (1.0 g, 5.46 mmol) and Et3N (552 mg, 5.46 mmol) in 25 mL of THF was cooled to 0° C. and ClCOOi-Bu (745 mg, 5.46 mmol) was added dropwise. After the addition was over, the reaction mixture was stirred for additional 5 min and then aq NH4OH (0.63 mL of 28% solution, 10.46 mmol) was added. After overnight stirring, the solvent was evaporated, the residue was taken up in water and basified to pH 9. The precipitated solid was filtered, washed with water and dried over P2O5 in a vacuum desiccator to provide 500 mg (48%) of the 4-(5-oxazolyl)-benzamide: 1H NMR (DMSO-d6) δ 8.50 (s, 1H), 8.20–7.80 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196078B2
Source datasetuspto-grants-2007_03
ORD IDord-1e3780851e8f4fb3a81767de4a3dec7b
Source noteuspto-grants-2007_03